villi have lots of capiliaries to help maintain conc gradient
villi have muscles which move to mix the contents of the ileum, helps maintain conc gradient
epithelial cells adaptations for digestion:
microvilli increase surface area
many mitochondria provide energy for active transport
carrier proteins for activetransport
channel proteins for facilitateddiffusion
amylase produced in smallintestine and pancreas
breaks glycosidic bonds in starch to form maltose
small intestine produces membrane bound disaccharides
maltase, sucrase, lactase
break glycosidic bonds to hydrolyse disaccharides into monosaccharides
glucose and galactose are actively transported using sodium ions through co-transporter proteins
fructose is absorbed by facilitateddiffusion trough a transporterprotein
cotransport (6)
sodium removed from epithelial cell by activetransport or the sodiumpotassium pump
into the blood
maintaining sodiumconcgradient between lumen and epithelial cell
via carrier or channel proteins
glycose moves into blood
by facilitated diffusion
break down of starch (5)
amylase from salivary glands/ pancreas breaks down
starch to maltose
maltase in small intestine
breaks maltose into glucose
glucose hydrolysed by hydrolysis of glycosidic bonds
peptidases are enzymes that breakown proteins in a series of hydrolysis reactions
there are 3 protease enzymes
endopeptidases hydrolyse peptide bonds within a large protein to create smaller polypeptide chains
create more terminal ends for exopeptidases to work on
exopeptidases hydrolyseterminalpeptide bonds to create smallerpolypeptide chains
dipeptidases located on the membrane of epithelial cells
work on dipeptides to hydrolyse peptide bonds
creates 2single amino acids which can be transported through the membrance into the epithelial cell
facilitated diffusion
no ATP needed
through carrier and channel proteins
active transport
uses ATP
simple diffusion
no ATP or transportprotein required
why exo and endopeptidases together is more efficient
-endo hydrolyse internalpeptide bonds
-creating more terminal ends and increasing surface area for exopeptidases
structure of proteins (6)
polymer of amino acids
joined by peptide bonds
formed by condensation reaction
primary structure is order of amino acids
secondary strucutre is folding of polypeptide chain due to hydrogen bonds into alpha helix or beta pleated sheet
tertiary structure is 3d foldinf due to hydrogen, ionic adn disulfide bonds
quaternary structure is 2 or more polypeptide chains
how proteins are digested in the gut (4)
endopeptidases break polypeptide into smaller chains
by hydrolysing internal peptide bonds
exopeptidases hydrolyse terminal peptide bonds
dipeptidases hydrolyses dipeptides into amino acids
lipases hydrolyseesterbonds in triglycerides to form fattyacids and monoglycerides
lipases are made in the pancreas and secreted into the smallintestine
bile salts produced in liver and stored in gallbladder which releases them into the smallintestine
bile salts help break down largefatglobules by emulsifying them into smallerdroplets. this speeds up lipases action by increasingsurfacearea of lipids exposed to the enzyme
digestion of lipids (6)
micelles contain bilesalts and fattyacids / monoglycerides
make fattyacids / monoglycerides more soluble and carry them to the lining of the ilium
absorbed by diffusion
triglycerides reformed in cells
vesicles move to cell membrane
once lipids are broken down into fattyacids and monoglycerides they stay attached to bile salts and form smaller structures called micelles
micelles
deliver fattyacids, glycerol and monoglycerides to epithelial cells of the ileum for absorption
water soluble vesicle formed of fatty acids, glycerol, monoglycerides and bilesalts
advantage of lipid droplet and micelle formation (3)
droplets increasesurfacearea for lipase
so fasterhydrolysis of triglycerides
micelles carry fattyacids and glycerol through the membrane of epithelial cell